Cannabinoids in anaesthesia and pain therapy

被引:17
作者
Azad, Shahnaz Christina [1 ,3 ]
Rammes, Gerhard [2 ,3 ]
机构
[1] Univ Munich, Klinikum Grosshadern, Dept Anaesthesiol, Pain Management Unit, D-80539 Munich, Germany
[2] Tech Univ Munich, Klinikum Rechts Isar, Dept Anaesthesiol, D-80290 Munich, Germany
[3] Max Planck Inst Psychiat, Clin Neuropharmacol Grp, D-80804 Munich, Germany
关键词
anaesthesia; cannabinoids; neuroplasticity; pain; spasticity;
D O I
10.1097/01.aco.0000174959.05383.9c
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Purpose of review Cannabinoids have been known for their analgesic, anxiolytic, antiemetic and antispastic properties for many centuries. Since an endogenous cannabinoid system has been identified in the past two decades, cannabinoids have also become the focus of interest in western medicine. This review summarizes preclinical and clinical studies on the role of the endocannabinoid system and exogenous cannabinoids in anaesthesia and pain management. Recent findings It has recently been shown that the endocannabinoid system is involved in the effects of the widely used anaesthetic drug propofol. In terms of nociception, preclinical data suggest that the endocannabinoid system plays an important role in the control of synaptic transmission and synaptic plasticity in pain pathways. In patients, the treatment of acute pain often requires relatively high doses of cannabinoids, which are associated with considerable side-effects such as dizziness and sedation. In contrast, preclinical and clinical data suggest that lower doses of cannabinoids may be effective for the treatment of allodynia and hyperalgesia in neuropathic pain. In multiple sclerosis, cannabinoids have been shown to have beneficial effects on spasticity, pain, tremor and bladder dysfunction. Summary In general, the results of the very few well-conducted clinical trials often diverge from the highly interesting and promising findings of preclinical studies. Taken together, the most recent preclinical and clinical data suggest that cannabinoids should be applied as low-dose co-analgesics to inhibit neuroplasticity and central sensitization rather than as analgesics in acute pain.
引用
收藏
页码:424 / 427
页数:4
相关论文
共 30 条
[1]   Are oral cannabinoids safe and effective in refractory neuropathic pain? [J].
Attal, N ;
Brasseur, L ;
Guirimand, D ;
Clermond-Griamien, S ;
Atlami, S ;
Bouhassira, D .
EUROPEAN JOURNAL OF PAIN, 2004, 8 (02) :173-177
[2]   Endogenous cannabinoid system. Effect on neuronal plasticity and pain memory [J].
Azad S.C. ;
Huge V. ;
Schöps P. ;
Hilf C. ;
Beyer A. ;
Dodt H.-U. ;
Rammes G. ;
Zieglgänsberger W. .
Der Schmerz, 2005, 19 (6) :521-527
[3]   Activation of the cannabinoid receptor type 1 decreases glutamatergic and GABAergic synaptic transmission in the lateral amygdala of the mouse [J].
Azad, SC ;
Eder, M ;
Marsicano, G ;
Lutz, B ;
Zieglgänsberger, W ;
Rammes, G .
LEARNING & MEMORY, 2003, 10 (02) :116-128
[4]   Neurogenic hyperalgesia versus painful hypoalgesia:: two distinct mechanisms of neuropathic pain [J].
Baumgärtner, U ;
Magerl, W ;
Klein, T ;
Hopf, HC ;
Treede, RD .
PAIN, 2002, 96 (1-2) :141-151
[5]   Synergistic interactions between cannabinoid and opioid analgesics [J].
Cichewicz, DL .
LIFE SCIENCES, 2004, 74 (11) :1317-1324
[6]   Repeated treatment with the synthetic cannabinoid WIN 55,212-2 reduces both hyperalgesia and production of pronociceptive mediators in a rat model of neuropathic pain [J].
Costa, B ;
Colleoni, M ;
Conti, S ;
Trovato, AE ;
Bianchi, M ;
Sotgiu, ML ;
Giagnoni, G .
BRITISH JOURNAL OF PHARMACOLOGY, 2004, 141 (01) :4-8
[7]   The endogenous cannabinoid system and its role in nociceptive behavior [J].
Cravatt, BF ;
Lichtman, AH .
JOURNAL OF NEUROBIOLOGY, 2004, 61 (01) :149-160
[8]   THE EFFICACY AND SAFETY OF NABILONE (A SYNTHETIC CANNABINOID) IN THE TREATMENT OF ANXIETY [J].
FABRE, LF ;
MCLENDON, D .
JOURNAL OF CLINICAL PHARMACOLOGY, 1981, 21 (8-9) :S377-S382
[9]   Role of endogenous cannabinoids in synaptic signaling [J].
Freund, TF ;
Katona, I ;
Piomelli, D .
PHYSIOLOGICAL REVIEWS, 2003, 83 (03) :1017-1066
[10]   Hypotensive effect of anandamide through the activation of CB1 and VR1 spinal receptors in urethane-anesthetized rats [J].
García, MD ;
Adler-Graschinsky, E ;
Celuch, SM .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2003, 368 (04) :270-276